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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226438Generated: October 30, 2026

Acetic Acid → HCID 9890404, compound

https://huagongshe.com/reaction/2226438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 53649395HCID 53649395—
ReactantHCID 178506676HCID 178506676—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9890404HCID 9890404—

Reaction Steps

476 mg of 6-(1-isoquinolyloxy)-4-methoxymethyl-9-tosyl-β-carboline-3-carboxylic acid isopropyl ester is mixed in 10 ml of tetrahydrofuran under argon at -60° C. with 0.79 ml of a 0.9 m solution of phenyllithium in benzene. After 1 hour at -60° C., it is stirred for 16 hours at room temperature. The batch is acidified with glacial acetic acid and concentrated by evaporation. The residue is dispersed in ethyl acetate/water and the organic phase is washed, dried, filtered and concentrated by evaporation in succession with respectively saturated sodium bicarbonate and common salt solution. The residue is chromatographed on silica gel with methylene chloride: ethanol=10:1. The corresponding fractions are combined, concentrated by evaporation and recrystallized. 30 mg of 6-(1-isoquinolyloxy)-4-methoxymethyl-3-benzoyl-β-carboline of melting point 159°-160° C. (ethyl acetate/hexane) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348958
Source datasetuspto-grants-1994_09
ORD IDord-ad6082d21c0342f39a321600a133c2d0
Source noteuspto-grants-1994_09